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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 325947Generated: October 26, 2026

Sulfuric Acid → 2,6-Dichlorobenzylglyoxal diethylacetal

https://huagongshe.com/reaction/325947

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
Reactant1-Bromomethyl-2,6-dichlorobenzeneHCID 30159—
ReactantMagnesiumHCID 5462224—
ReactantDiethoxyacetic acid piperidinyl amideHCID 54475451—
SolventDiethyl EtherHCID 3283—
Product2,6-Dichlorobenzylglyoxal diethylacetalHCID 20463294—

Reaction Steps

2.4 g of magnesium turnings are covered with 100 ml of dry diethyl ether. To that mixture is then added dropwise a solution of 24 g of 2,6-dichlorobenzylbromide in 50 ml of dry diethyl ether at such a rate that a smooth reaction is maintained. After the addition is complete, the reaction mixture is refluxed for one additional hour, then is cooled to room temperature. The reaction mixture is then added dropwise, over a period of 2 hours, to a cooled (0°-5° C.) solution of diethyoxyacetic acid piperidinyl amide (21.5 g) in 100 ml of diethyl ether. After the addition is complete, the reaction mixture is stirred for an additional hour at 5° C. The mixture is then poured into cold sulfuric acid (400 ml of water containing 30 ml of concentrated sulfuric acid). The ether layer is separated and evaporated to dryness. The residue, which consists of crude 2,6-dichlorobenzylglyoxal diethylacetal, is distilled under reduced pressure (130°-140° C./1 mmHg) and used in Example 49(b) and 50(a) set forth below.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04443466
Source datasetuspto-grants-1984_04
ORD IDord-65aacbeed2234742939fcf83f9172270
Source noteuspto-grants-1984_04